Cytosolic acetyl-CoA promotes histone acetylation predominantly at H3K27 in Arabidopsis
Journal
Nature Plants
Journal Volume
3
Journal Issue
10
Pages
814-824
Date Issued
2017
Author(s)
Chen C.
Li C.
Wang Y.
Renaud J.
Tian G.
Kambhampati S.
Saatian B.
Nguyen V.
Hannoufa A.
Marsolais F.
Yuan Z.-C.
Yu K.
Austin R.S.
Liu J.
Kohalmi S.E.
Huang S.
Cui Y.
Abstract
Acetyl-coenzyme A (acetyl-CoA) is a central metabolite and the acetyl source for protein acetylation, particularly histone acetylation that promotes gene expression. However, the effect of acetyl-CoA levels on histone acetylation status in plants remains unknown. Here, we show that malfunctioned cytosolic acetyl-CoA carboxylase1 (ACC1) in Arabidopsis leads to elevated levels of acetyl-CoA and promotes histone hyperacetylation predominantly at lysine 27 of histone H3 (H3K27). The increase of H3K27 acetylation (H3K27ac) is dependent on adenosine triphosphate (ATP)-citrate lyase which cleaves citrate to acetyl-CoA in the cytoplasm, and requires histone acetyltransferase GCN5. A comprehensive analysis of the transcriptome and metabolome in combination with the genome-wide H3K27ac profiles of acc1 mutants demonstrate the dynamic changes in H3K27ac, gene transcripts and metabolites occurring in the cell by the increased levels of acetyl-CoA. This study suggests that H3K27ac is an important link between cytosolic acetyl-CoA level and gene expression in response to the dynamic metabolic environments in plants. ? 2017 The Author(s).
Type
journal article